MY105308A - Imadazo[4,5-b]quinoloxyalkanoic acid amides with enhanced water solubility. - Google Patents
Imadazo[4,5-b]quinoloxyalkanoic acid amides with enhanced water solubility.Info
- Publication number
- MY105308A MY105308A MYPI90001900A MYPI19901900A MY105308A MY 105308 A MY105308 A MY 105308A MY PI90001900 A MYPI90001900 A MY PI90001900A MY PI19901900 A MYPI19901900 A MY PI19901900A MY 105308 A MY105308 A MY 105308A
- Authority
- MY
- Malaysia
- Prior art keywords
- carbon atoms
- alkyl
- cycloalkyl
- acid amides
- water solubility
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
A NOVEL SERIES OF 2, 3-DIHYDRO-2-OXO-1H-IMIDAZO- [4, 5-B] QUINOLINYLOXYALKANOIC ACID AMIDES HAVING ENHANCED WATER SOLUBILITY IS DISCLOSED OF THE FORMULA WHEREIN N IS 3 TO 5; R1 IS ALKYL OF 1 TO 4 CARBON ATOMS; R2 IS HYDROGEN; R3 IS 1-PIPERIDINYLETHYL, 1-BENZYLPIPERIDIN-4-YL, 4-(1-PIPERIDINYL) PIPERIDINE, (1-ALKYL-2-PYRROLIDINYL) -ALKYL WHERE ALKYL IS 1 TO 4 CARBON ATOMS, 3-QUINUCLIDINYL; R2 AND R3 TOGETHER WITH THE NITROGEN ATOM TO WHICH THEY ARE ATTACHED FORM 4-R4-PIPERAZIN-1-YL WHEREIN R4 IS ALKYL OF 1 TO 7 CARBON ATOMS, ALKOXYETHYL OF 3 TO 7 CARBON ATOMS, PYRIDINYL, PYRIMIDINYL, TETRAHYDROPYRANYLMETHYL, THIENYLMETHYL, CYCLOALKYL- (CH2)M WHERE M IS ZERO OR ONE AND CYCLOALKYL IS 5 TO 7 CARBON ATOMS EXCEPT M IS ZERO WHEN CYCLOALKYL IS 7 CARBON ATOMS, BENZYL, 4-FLUOROBENZYL, 3-TRIFLUOROMETHYLBENZYL, 4-ALKOXYBENZYL WHERE ALKOXY IS 1 TO 4 CARBON ATOMS. THE COMPOUNDS ARE CYCLIC AMP PHOSPHODIESTERASE INHIBITORS AND ARE PARTICULARLY USEFUL AS INHIBITORS OF BLOOD PLATELET AGGREGATION AND/OR AS CARDIOTONIC AGENTS.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/430,228 US4943573A (en) | 1989-11-01 | 1989-11-01 | Imidazo[4,5-b]quinolinyloxyalkanoic acid amides with enhanced water solubility |
Publications (1)
Publication Number | Publication Date |
---|---|
MY105308A true MY105308A (en) | 1994-09-30 |
Family
ID=23706624
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MYPI90001900A MY105308A (en) | 1989-11-01 | 1990-10-30 | Imadazo[4,5-b]quinoloxyalkanoic acid amides with enhanced water solubility. |
Country Status (20)
Country | Link |
---|---|
US (1) | US4943573A (en) |
EP (1) | EP0426180A3 (en) |
JP (1) | JPH03169880A (en) |
KR (1) | KR910009705A (en) |
CN (1) | CN1025999C (en) |
AU (1) | AU639033B2 (en) |
CA (1) | CA2027935A1 (en) |
EG (1) | EG19372A (en) |
FI (1) | FI92697C (en) |
HU (1) | HU209305B (en) |
IE (1) | IE61579B1 (en) |
IL (1) | IL96167A (en) |
MY (1) | MY105308A (en) |
NO (1) | NO175531C (en) |
NZ (1) | NZ235868A (en) |
OA (1) | OA09323A (en) |
PT (1) | PT95765A (en) |
RU (1) | RU2041210C1 (en) |
YU (1) | YU205590A (en) |
ZA (1) | ZA908725B (en) |
Families Citing this family (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4943573A (en) * | 1989-11-01 | 1990-07-24 | Bristol-Myers Squibb Company | Imidazo[4,5-b]quinolinyloxyalkanoic acid amides with enhanced water solubility |
PH31245A (en) * | 1991-10-30 | 1998-06-18 | Janssen Pharmaceutica Nv | 1,3-Dihydro-2H-imidazoÄ4,5-BÜ-quinolin-2-one derivatives. |
US5552267A (en) * | 1992-04-03 | 1996-09-03 | The Trustees Of Columbia University In The City Of New York | Solution for prolonged organ preservation |
US5158958A (en) * | 1992-04-03 | 1992-10-27 | Bristol-Myers Squibb Company | Imidazo[4,5-b]quinolinyl oxy alkyl sulfonyl piperidine derivatives |
US5196428A (en) * | 1992-04-03 | 1993-03-23 | Bristol-Myers Squibb Company | Imidazo[4,5-b]qinolinyl oxy alkyl ureas |
US5208237A (en) * | 1992-04-03 | 1993-05-04 | Bristol-Meyers Squibb Company | 7-oxypropylsulfonamido-imidazo[4,5-b]quinolin-2-ones |
US5348960A (en) * | 1992-04-03 | 1994-09-20 | Bristol-Myers Squibb Company | Imidazo[4,5-b]quinolinyl oxy alkyl tetrazolyl piperidine derivatives |
TW593317B (en) * | 1993-06-21 | 2004-06-21 | Janssen Pharmaceutica Nv | Positive cardiac inotropic and lusitropic pyrroloquinolinone derivatives |
US5672622A (en) * | 1994-04-21 | 1997-09-30 | Berlex Laboratories, Inc. | Treatment of multiple sclerosis |
US6060501A (en) * | 1994-06-02 | 2000-05-09 | Schering Aktiengesellschaft | Combined treatment of multiple sclerosis |
WO1996005202A1 (en) * | 1994-08-17 | 1996-02-22 | Nippon Hypox Laboratories Inc. | Imidazoquinoline derivative |
US5798767A (en) * | 1996-03-15 | 1998-08-25 | Rendition, Inc. | Method and apparatus for performing color space conversion using blend logic |
SE9902987D0 (en) * | 1999-08-24 | 1999-08-24 | Astra Pharma Prod | Novel compounds |
US20030186963A1 (en) * | 2001-09-14 | 2003-10-02 | Dorwald Florencio Zaragoza | Substituted piperidines |
WO2003031432A1 (en) * | 2001-10-12 | 2003-04-17 | Novo Nordisk A/S | Substituted piperidines and their use for the treatment of diseases related to the histamine h3 receptor |
US7064135B2 (en) | 2001-10-12 | 2006-06-20 | Novo Nordisk Inc. | Substituted piperidines |
US7772188B2 (en) | 2003-01-28 | 2010-08-10 | Ironwood Pharmaceuticals, Inc. | Methods and compositions for the treatment of gastrointestinal disorders |
EP2275095A3 (en) | 2005-08-26 | 2011-08-17 | Braincells, Inc. | Neurogenesis by muscarinic receptor modulation |
EP2258359A3 (en) | 2005-08-26 | 2011-04-06 | Braincells, Inc. | Neurogenesis by muscarinic receptor modulation with sabcomelin |
US7985756B2 (en) | 2005-10-21 | 2011-07-26 | Braincells Inc. | Modulation of neurogenesis by PDE inhibition |
EP1942879A1 (en) | 2005-10-31 | 2008-07-16 | Braincells, Inc. | Gaba receptor mediated modulation of neurogenesis |
US20100216734A1 (en) | 2006-03-08 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis by nootropic agents |
MX2008014320A (en) | 2006-05-09 | 2009-03-25 | Braincells Inc | 5 ht receptor mediated neurogenesis. |
JP2009536669A (en) | 2006-05-09 | 2009-10-15 | ブレインセルス,インコーポレイティド | Neurogenesis by angiotensin regulation |
US8227603B2 (en) * | 2006-08-01 | 2012-07-24 | Cytokinetics, Inc. | Modulating skeletal muscle |
US8299248B2 (en) * | 2006-08-02 | 2012-10-30 | Cytokinetics, Incorporated | Certain 1H-imidazo[4,5-b]pyrazin-2(3H)-ones and 1H-imidazo[4,5-b]pyrazin-2-ols and methods for their use |
WO2008016669A2 (en) * | 2006-08-02 | 2008-02-07 | Cytokinetics, Incorporated | Certain chemical entities, compositions and methods |
JP2010502722A (en) | 2006-09-08 | 2010-01-28 | ブレインセルス,インコーポレイティド | Combinations containing 4-acylaminopyridine derivatives |
US20100184806A1 (en) | 2006-09-19 | 2010-07-22 | Braincells, Inc. | Modulation of neurogenesis by ppar agents |
EP2139478A4 (en) * | 2007-03-30 | 2010-05-05 | Cytokinetics Inc | Certain chemical entities, compositions and methods |
WO2008151257A2 (en) | 2007-06-04 | 2008-12-11 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders |
US8969514B2 (en) | 2007-06-04 | 2015-03-03 | Synergy Pharmaceuticals, Inc. | Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases |
GB0808968D0 (en) * | 2008-05-16 | 2008-06-25 | Shire Llc | Substitute quinazolines |
GB0808952D0 (en) * | 2008-05-16 | 2008-06-25 | Shire Llc | Substituted quinazolines |
GB0808947D0 (en) * | 2008-05-16 | 2008-06-25 | Shire Llc | Substituted quinazolines |
GB0808967D0 (en) * | 2008-05-16 | 2008-06-25 | Shire Llc | Substitute quinazolines |
AU2009256157B2 (en) | 2008-06-04 | 2014-12-18 | Bausch Health Ireland Limited | Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders |
EP2321341B1 (en) | 2008-07-16 | 2017-02-22 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase useful for the treatment of gastrointestinal, inflammation, cancer and other disorders |
US20100216805A1 (en) | 2009-02-25 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis using d-cycloserine combinations |
US9616097B2 (en) | 2010-09-15 | 2017-04-11 | Synergy Pharmaceuticals, Inc. | Formulations of guanylate cyclase C agonists and methods of use |
EA201391254A1 (en) | 2011-03-01 | 2014-02-28 | Синерджи Фармасьютикалз Инк. | METHOD FOR OBTAINING GUANYLATZCLAZE AGONISTS C |
SG10201605707UA (en) | 2011-07-13 | 2016-09-29 | Cytokinetics Inc | Combination als therapy |
EP2804603A1 (en) | 2012-01-10 | 2014-11-26 | President and Fellows of Harvard College | Beta-cell replication promoting compounds and methods of their use |
CA2902348C (en) | 2013-02-25 | 2021-11-30 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase and their uses |
WO2014151206A1 (en) | 2013-03-15 | 2014-09-25 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase and their uses |
AU2014235209B2 (en) | 2013-03-15 | 2018-06-14 | Bausch Health Ireland Limited | Guanylate cyclase receptor agonists combined with other drugs |
WO2014197720A2 (en) | 2013-06-05 | 2014-12-11 | Synergy Pharmaceuticals, Inc. | Ultra-pure agonists of guanylate cyclase c, method of making and using same |
US20160184387A1 (en) | 2013-08-09 | 2016-06-30 | Dominique Charmot | Compounds and methods for inhibiting phosphate transport |
CN114340631A (en) | 2019-05-21 | 2022-04-12 | 阿德利克斯股份有限公司 | Combination for reducing serum phosphate in a patient |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3932407A (en) * | 1973-11-19 | 1976-01-13 | Bristol-Myers Company | Optionally substituted 1,2,3,5-tetrahydroimidezo(2,1-b)-quinazolin-2-ones and 6(H)-1,2,3,4-tetrahydropyimido(2,1-b)quinazolin-2-ones |
NL7807507A (en) * | 1977-07-25 | 1979-01-29 | Hoffmann La Roche | TRICYCLICAL CONNECTIONS. |
US4490371A (en) * | 1983-02-16 | 1984-12-25 | Syntex (U.S.A.) Inc. | N,N-Disubstituted-(2-oxo-1,2,3,5-tetrahydroimidazo-[2,1-B]quinazolinyl)oxyalkylamides |
JPS60193991A (en) * | 1984-02-15 | 1985-10-02 | シンテツクス(ユー・エス・エイ)インコーポレイテツド | Imidazoquinazolinyloxyalkylamide derivative |
US4668686A (en) * | 1985-04-25 | 1987-05-26 | Bristol-Myers Company | Imidazoquinoline antithrombrogenic cardiotonic agents |
US4775674A (en) * | 1986-05-23 | 1988-10-04 | Bristol-Myers Company | Imidazoquinolinylether derivatives useful as phosphodiesterase and blood aggregation inhibitors |
US4701459A (en) * | 1986-07-08 | 1987-10-20 | Bristol-Myers Company | 7-amino-1,3-dihydro-2H-imidazo[4,5-b]quinolin 2-ones and method for inhibiting phosphodiesterase and blood platelet aggregation |
US4943573A (en) * | 1989-11-01 | 1990-07-24 | Bristol-Myers Squibb Company | Imidazo[4,5-b]quinolinyloxyalkanoic acid amides with enhanced water solubility |
-
1989
- 1989-11-01 US US07/430,228 patent/US4943573A/en not_active Expired - Fee Related
-
1990
- 1990-10-18 CA CA002027935A patent/CA2027935A1/en not_active Abandoned
- 1990-10-29 NZ NZ235868A patent/NZ235868A/en unknown
- 1990-10-29 FI FI905326A patent/FI92697C/en not_active IP Right Cessation
- 1990-10-30 IL IL9616790A patent/IL96167A/en not_active IP Right Cessation
- 1990-10-30 NO NO904689A patent/NO175531C/en unknown
- 1990-10-30 JP JP2290987A patent/JPH03169880A/en active Pending
- 1990-10-30 YU YU205590A patent/YU205590A/en unknown
- 1990-10-30 MY MYPI90001900A patent/MY105308A/en unknown
- 1990-10-31 IE IE392390A patent/IE61579B1/en not_active IP Right Cessation
- 1990-10-31 AU AU65679/90A patent/AU639033B2/en not_active Ceased
- 1990-10-31 OA OA59882A patent/OA09323A/en unknown
- 1990-10-31 EP EP19900120952 patent/EP0426180A3/en not_active Ceased
- 1990-10-31 ZA ZA908725A patent/ZA908725B/en unknown
- 1990-10-31 RU SU904831618A patent/RU2041210C1/en active
- 1990-10-31 CN CN90108762A patent/CN1025999C/en not_active Expired - Fee Related
- 1990-10-31 PT PT95765A patent/PT95765A/en not_active Application Discontinuation
- 1990-10-31 KR KR1019900017645A patent/KR910009705A/en not_active Application Discontinuation
- 1990-11-01 EG EG65590A patent/EG19372A/en active
- 1990-11-01 HU HU906977A patent/HU209305B/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
JPH03169880A (en) | 1991-07-23 |
NO904689L (en) | 1991-05-02 |
RU2041210C1 (en) | 1995-08-09 |
US4943573A (en) | 1990-07-24 |
NO904689D0 (en) | 1990-10-30 |
HU209305B (en) | 1994-04-28 |
OA09323A (en) | 1992-09-15 |
HU906977D0 (en) | 1991-05-28 |
EP0426180A2 (en) | 1991-05-08 |
PT95765A (en) | 1991-09-13 |
ZA908725B (en) | 1991-07-31 |
IL96167A0 (en) | 1991-07-18 |
FI905326A0 (en) | 1990-10-29 |
KR910009705A (en) | 1991-06-28 |
FI92697B (en) | 1994-09-15 |
EG19372A (en) | 1994-12-30 |
CN1025999C (en) | 1994-09-28 |
CN1051359A (en) | 1991-05-15 |
EP0426180A3 (en) | 1992-01-08 |
AU6567990A (en) | 1991-05-23 |
NO175531C (en) | 1994-10-26 |
YU205590A (en) | 1992-09-07 |
IL96167A (en) | 1994-11-11 |
IE903923A1 (en) | 1991-05-08 |
HUT56102A (en) | 1991-07-29 |
CA2027935A1 (en) | 1991-05-02 |
FI92697C (en) | 1994-12-27 |
AU639033B2 (en) | 1993-07-15 |
IE61579B1 (en) | 1994-11-16 |
NZ235868A (en) | 1993-12-23 |
NO175531B (en) | 1994-07-18 |
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